InCl3 catalyzed three-component synthesis of α-benzylamino coumarins and diketones
-
Add time:08/30/2019 Source:sciencedirect.com
A convenient and practical InCl3 catalyzed three-component reaction of 4-hydroxy coumarin/1,3 diones, aromatic aldehyde, and secondary amine for the synthesis of α-benzylamino coumarins and diketones in good yields has been reported.
We also recommend Trading Suppliers and Manufacturers of 4-(BENZYLAMINO)-2-OXO-2H-CHROMENE-3-CARBALDEHYDE (cas 111222-25-4). Pls Click Website Link as below: cas 111222-25-4 suppliers
Prev:Synthesis and evaluation of substituted 4-(N-benzylamino)cinnamate esters as potential anti-cancer agents and HIV-1 integrase inhibitors
Next:Discovery of novel substituted benzo-anellated 4-benzylamino pyrrolopyrimidines as dual EGFR and VEGFR2 inhibitors) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Antimalarial 3-arylamino-6-benzylamino-1,2,4,5-tetrazines09/06/2019
- Potential-dependant SERS interaction of ortho-substituted N-benzylamino(boronphenyl)methylphosphonic acid with Ag, Au, and Cu electrode surfaces☆09/05/2019
- 1-[4-(N-Benzylamino)phenyl]-3-phenylurea derivatives as a new class of hypoxia-inducible factor-1α inhibitors09/04/2019
- Investigation of adsorption mode of a novel group of N-benzylamino(boronphenyl)methylphosphonic acids using SERS09/03/2019
- Boron tribromide mediated debenzylation of benzylamino and benzyloxy groups09/02/2019
- Conformation and photochemical properties of 3-benzoyl-4-benzylamino-7-dimethylaminocoumarin09/01/2019
- Discovery of novel substituted benzo-anellated 4-benzylamino pyrrolopyrimidines as dual EGFR and VEGFR2 inhibitors08/31/2019
- Synthesis and evaluation of substituted 4-(N-benzylamino)cinnamate esters as potential anti-cancer agents and HIV-1 integrase inhibitors08/29/2019


